Canonical Allele Identifier: CA343771993

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873031T>A (hg19) ; chr1:g.173903893T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903893T>A , CM000663.2:g.173903893T>A	GRCh38
NC_000001.10:g.173873031T>A , CM000663.1:g.173873031T>A	GRCh37
NC_000001.9:g.172139654T>A	NCBI36
NG_012462.1:g.18486A>T , LRG_577:g.18486A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1391A>T MANE Select	ENSP00000356671.3:p.Lys464Met
ENST00000367698.3:c.1391A>T	ENSP00000356671.3:p.Lys464Met
ENST00000617423.4:c.776A>T	ENSP00000478688.1:p.Lys259Met
NM_000488.3:c.1391A>T , LRG_577t1:c.1391A>T	NP_000479.1:p.Lys464Met
XM_005245198.2:c.1247A>T	XP_005245255.1:p.Lys416Met
NM_001365052.1:c.1247A>T	NP_001351981.1:p.Lys416Met
NM_000488.4:c.1391A>T MANE Select	NP_000479.1:p.Lys464Met
NM_001365052.2:c.1247A>T	NP_001351981.1:p.Lys416Met
NM_001386302.1:c.1514A>T	NP_001373231.1:p.Lys505Met
NM_001386303.1:c.1472A>T	NP_001373232.1:p.Lys491Met
NM_001386304.1:c.1370A>T	NP_001373233.1:p.Lys457Met
NM_001386305.1:c.1334A>T	NP_001373234.1:p.Lys445Met
NM_001386306.1:c.1175A>T	NP_001373235.1:p.Lys392Met